WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype

被引：38
|
作者：
Faqeih, Eissa [1 ]
Shaheen, Ranad [2 ]
Alkuraya, Fowzan S. [2 ,3 ]
机构：
[1] King Fahad Med City, Dept Pediat, Riyadh, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia
[3] Alfaisal Univ, Coll Med, Dept Anat & Cell Biol, Riyadh, Saudi Arabia
来源：
JOURNAL OF MEDICAL GENETICS | 2013年 / 50卷 / 07期
关键词：
D O I：
10.1136/jmedgenet-2013-101750
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：491 / 492
页数：2
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